A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual

被引:0
|
作者
Lyu, Hongjuan [1 ]
Wang, Kun [1 ]
Feng, Zhihui [2 ]
Xu, Tao [3 ,4 ]
机构
[1] Qingdao Women & Childrens Hosp, Obstet Dept, Qingdao, Peoples R China
[2] Qingdao Blood Ctr, Inst Transfus Med, Qingdao, Peoples R China
[3] Qingdao Women & Childrens Hosp, Urol Dept, Qingdao, Peoples R China
[4] Qingdao Women & Childrens Hosp, Urol Dept, 6 Tongfu Rd, Qingdao 266071, Shandong, Peoples R China
关键词
D O I
10.1111/trf.17820
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:E18 / E20
页数:3
相关论文
共 50 条
  • [31] A novel B allele with c.736T>C, c.738C>A, and c.930A>G variations identified in a Chinese individual with Bw phenotype
    Zhang, Bing
    Hong, Xiaozhen
    Xu, Xianguo
    Zhu, Faming
    TRANSFUSION, 2023, 63 (04) : E25 - E26
  • [32] A novel RHD allele, with c.491A > T (p.Asp164Val) mutation, identified via family pedigree analysis
    Wang, Jing
    Que, Wenjun
    Xing, Yan
    Li, Qing
    Zhan, Tingxi
    Yu, Zebo
    TRANSFUSION, 2021, 61 (06) : E46 - E48
  • [33] Two novelAalleles with c.322C>T or c.410C>Tmutations on the ABO*A1.02 allele were identified in the Chinese individuals
    Hong, Xiaozhen
    Zhang, Jingjing
    Ying, Yanling
    He, Ji
    Zhu, Faming
    TRANSFUSION, 2020, 60 (10) : E38 - E39
  • [34] Identification of a novel A allele with a c.423 C > A mutation on the ABO*A1.02 allele
    He, Yunlei
    Zhang, Jiwei
    Yu, Lu
    Shen, Longqiang
    Zhong, Fade
    Deng, Gang
    TRANSFUSION, 2022, 62 (07) : E32 - E33
  • [35] A novel RHD allele caused by RHD c.710_713dup associated with a negative phenotype in a Chinese Han blood donor
    Wu, Fan
    Zhuang, Nai-Bao
    Liang, Shuang
    Peng, Long
    Liang, Yan-lian
    Su, Yu-qing
    TRANSFUSION, 2022, 62 (08) : E40 - E42
  • [36] A novel RHD allele caused by c.687_689delAAG variant
    Shen, Yuqing
    Chen, Yuzi
    Yang, Xiaojun
    Gong, Junshun
    Wang, Yuanyuan
    Su, Naizhu
    TRANSFUSION, 2023, 63 (11) : E53 - E55
  • [37] Prenatal diagnosis of a rare β-thalassemia gene - 90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--SEA/-α4.2)
    Qian, Hou
    Huang, Jianlin
    Xu, Ji
    Zhao, Weihua
    Ye, Xiufeng
    Liu, Wenlan
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (11):
  • [38] Identification of a novel DEL allele with c.411G>C on the RHD01EL.01 allele background
    Shao, Lin-Nan
    Xia, Yue-Xin
    Li, Chun-Xiang
    Yang, Yi-Cheng
    Zhou, Shi-Hang
    TRANSFUSION, 2024, 64 (06) : E26 - E27
  • [39] Molecular and Family Analyses of a Novel RHD1058G>C Allele in a Chinese RhD Population
    Wang, Yueping
    Zhou, Rong
    Hong, Wo-Xia
    Wang, Xuedong
    Zhang, Ziyun
    Gu, Juan
    Wang, Xinping
    Wu, Chang-Lin
    Shao, Chaopeng
    CLINICAL LABORATORY, 2024, 70 (03) : 614 - 617
  • [40] Identification of a novel A allele with c.478C>T missense mutation on the ABO*A1.02 background
    Deng, Danfei
    Deng, Gang
    He, Yunlei
    Yu, Yong
    TRANSFUSION, 2022, 62 (09) : E47 - E48